This is highlighted by the defects observed in patients with mutations in either STIM1 or Orai1—which phenocopy each other—including severe combined immunodeficiency, muscle hypotonia, ectodermal dysplasia, and anhidrosis with dry skin and heat intolerance (Lacruz and Feske, 2015; McCarl et al., 2009). This evidence concerns the gene STIM1 and anhidrosis.